金黄色葡萄球菌
枯草芽孢杆菌
抗菌活性
大肠杆菌
咔唑
部分
化学
最小抑制浓度
细菌
微生物学
醌
立体化学
生物
抗生素
有机化学
生物化学
遗传学
基因
作者
Biswanath Chakraborty,Suchandra Chakraborty,Chandan Saha
摘要
The antibacterial activity of Murrayaquinone A ( 10 ), a naturally occurring carbazoloquinone alkaloid, and 6-methoxy-3,7-dimethyl-2,3-dihydro-1 H -carbazole-1,4(9 H )-dione ( 11 ), a synthetic carbazoloquinone, both obtained during the development of the synthesis of Carbazomycin G, having unique quinone moiety, was studied against Gram-positive ( Bacillus subtilis and Staphylococcus aureus ) and Gram-negative ( Escherichia coli and Pseudomonas sp.) bacteria. Compound 10 showed antibacterial activities against both of Escherichia coli and Staphylococcus aureus whereas compound 11 indicated the activity against Staphylococcus aureus only. Both compounds 10 and 11 exhibited minimum inhibitory concentration (MIC) of 50 μ g mL −1 against Staphylococcus aureus .
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